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Factors associated with pulmonary function decline of patients in the cystic fibrosis registry of Turkey: A retrospective cohort study

dc.contributor.authorEmiralioglu, Nagehan
dc.contributor.authorCakir, Banu
dc.contributor.authorSertcelik, Ahmet
dc.contributor.authorYalcin, Ebru
dc.contributor.authorKiper, Nural
dc.contributor.authorSen, Velat
dc.contributor.authorAltintas, Derya Ufuk
dc.contributor.authorSerbes, Mahir
dc.contributor.authorCokugras, Haluk
dc.contributor.authorKilinc, Ayse Ayzit
dc.contributor.authorBaskan, Azer Kilic
dc.contributor.authorHepkaya, Evrim
dc.contributor.authorYazan, Hakan
dc.contributor.authorTurel, Ozden
dc.contributor.authorKafi, Hale Molla
dc.contributor.authorYilmaz, Asli Imran
dc.contributor.authorUnal, Gokcen
dc.contributor.authorCaglar, Tugce
dc.contributor.authorDamadoglu, Ebru
dc.contributor.authorIrmak, Ilim
dc.contributor.authorDemir, Esen
dc.contributor.authorOzturk, Gokcen
dc.contributor.authorBingol, Aysen
dc.contributor.authorBasaran, Erdem
dc.contributor.authorSapan, Nihat
dc.contributor.authorAslan, Ayse Tana
dc.contributor.authorAsfuroglu, Pelin
dc.contributor.authorHarmanci, Koray
dc.contributor.authorKose, Mehmet
dc.contributor.authorHangul, Melih
dc.contributor.authorOzdemir, Ali
dc.contributor.authorTugcu, Gokcen
dc.contributor.authorPolat, Sanem Eryilmaz
dc.contributor.authorOzcan, Gizem
dc.contributor.authorGayretli, Zeynep Gokce
dc.contributor.authorKeskin, Ozlem
dc.contributor.authorBilgic, Sevgi
dc.contributor.authorYuksel, Hasan
dc.contributor.authorOzdogan, Sebnem
dc.contributor.authorTopal, Erdem
dc.contributor.authorCaltepe, Gonul
dc.contributor.authorCan, Demet
dc.contributor.authorEkren, Pervin Korkmaz
dc.contributor.authorKilic, Mehmet
dc.contributor.authorSuleyman, Ayse
dc.contributor.authorEyuboglu, Tugba Sismanlar
dc.contributor.authorCinel, Guzin
dc.contributor.authorPekcan, Sevgi
dc.contributor.authorCobanoglu, Nazan
dc.contributor.authorCakir, Erkan
dc.contributor.authorOzcelik, Ugur
dc.contributor.authorDogru, Deniz
dc.contributor.buuauthorSAPAN, NİHAT
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentPediatri Alerji Bölümü
dc.contributor.researcheridFUI-8766-2022
dc.date.accessioned2025-02-13T07:55:15Z
dc.date.available2025-02-13T07:55:15Z
dc.date.issued2024-07-09
dc.description.abstractBackground: The decline in pulmonary function is a predictor of disease progression in patients with cystic fibrosis (CF). This study aimed to determine the decline rate of percent predicted forced expiratory volume in 1 s (ppFEV1) based on the data of the CF Registry of Turkey. The secondary aim was to investigate the risk factors related to the decline in ppFEV1. Methods: A retrospective cohort study of CF patients over 6 years old, with pulmonary function data over at least 2 years of follow-up was extracted from the national CF registry for years 2017-2019. Patients were classified according to disease severity and age groups. Multivariate analysis was used to predict the decline in ppFEV1 and to investigate the associated risk factors. Results: A total of 1722 pulmonary function test results were available from 574 patients over the study period. Mean diagnostic age was older and weight for age, height for age, and body mass index z scores were significantly lower in the group of ppFEV1 < 40, while chronic Pseudomonas aeruginosa (p < .001) and mucoid P. aeruginosa colonization (p < .001) were significantly higher in this group (p < .001). Overall mean annual ppFEV1 decline was -0.97% (95% confidence interval [CI] = -0.02 to -1.92%). The mean change of ppFEV1 was significantly higher in the group with ppFEV1 >= 70 compared with the other (ppFEV1 < 40 and ppFEV1: 40-69) two groups (p = .004). Chronic P. aeruginosa colonization (odds ratio [OR] = 1.79 95% CI = 1.26-2.54; p = .01) and initial ppFEV1 >= 70 (OR = 2.98 95% CI = 1.06-8.36), p = .038) were associated with significant ppFEV1 decline in the whole cohort. Conclusions: This data analysis recommends close follow-up of patients with normal initial ppFEV1 levels at baseline; advocates for early interventions for P. aeruginosa; and underlines the importance of nutritional interventions to slow down lung disease progression.
dc.identifier.doi10.1002/ppul.27165
dc.identifier.eissn1099-0496
dc.identifier.endpage2966
dc.identifier.issn8755-6863
dc.identifier.issue11
dc.identifier.scopus2-s2.0-85197756695
dc.identifier.startpage2956
dc.identifier.urihttps://doi.org/10.1002/ppul.27165
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1002/ppul.27165
dc.identifier.urihttps://hdl.handle.net/11452/50354
dc.identifier.volume59
dc.identifier.wos001268137200001
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherWiley
dc.relation.journalPediatric Pulmonology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectLung-function decline
dc.subjectFev1 decline
dc.subjectRisk-factors
dc.subjectAdults
dc.subjectAdolescence
dc.subjectProgression
dc.subjectChildren
dc.subjectCystic fibrosis
dc.subjectFev1
dc.subjectPulmonary function test
dc.subjectPseudomonas aeruginosa
dc.subjectScience & technology
dc.subjectLife sciences & biomedicine
dc.subjectPediatrics
dc.subjectRespiratory system
dc.titleFactors associated with pulmonary function decline of patients in the cystic fibrosis registry of Turkey: A retrospective cohort study
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Pediatri Alerji Bölümü
local.indexed.atWOS
local.indexed.atScopus
relation.isAuthorOfPublicationcc312521-b6b8-4031-a0a0-b06b35291a1c
relation.isAuthorOfPublication.latestForDiscoverycc312521-b6b8-4031-a0a0-b06b35291a1c

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